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Development of Anode Materials for Solid Oxide Fuel Cells A Review

机译:固体氧化物燃料电池阳极材料的研究进展

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Solid oxide fuel cells (SOFCs) are electrochemical devices that provide significant advantages over the conventional power generation resources. Despite all these firm advantages there still remain a number of hurdles that have to be crossed before moving on for the viable commercialization of the solid oxide fuel cells (SOFCs). Most important of these hurdles primarily include the working temperature zone, proper materials selection for the electrodes, electrolytes, interconnects and the compatibility of the components! In this review, primarily the materials properties of the anodes are being evaluated and the mixed ionic electronic conductors (MIECs) being explored as the most probable candidates. Different constraints on the MIECs are outlined, and the possible paths to an improved anode are portrayed. The present situation is forcing the SOFC community to explore electronically conductive composites capable of conducting ionic species (MIECs) also at the anode. Most MIEC perovskites facilitate oxide-ion conduction via oxygen vacancies, whereas La{sub}(1-x)Sr{sub}xTiO{sub}(3+δ) have a few mobile oxygen vacancies in the perovskite matrix. The ionic conductivity of Sr{sub}2Mg{sub}(1-x)Mn{sub}xMoO{sub}(6-δ) is ~10 S/cm at 8000℃ in H{sub}2 and the system gives sulfur tolerance and excellent anode performance. La{sub}0.8Sr{sub}0.2Ga{sub}0.83Mg{sub}0.17O{sub}2.815 (LSGM) was used as electrolyte and SrCo{sub}0.8Fe{sub}0.2O{sub}(3-δ) as cathode in a system and the maximum power density(P{sub}(max)) achieved was 0.84 Wcm{sup}(-2) at 8000℃ and 0.45 Wcm{sup}(-2) at 7000℃ resp. in H{sub}2. The addition of Rh as a noble metal to a Cu/SDC anode improved the cell performance significantly in methane. Ce{sub}0.84Ti{sub}0.15Pt{sub}0.01O{sub}(2-δ) has shown good reducibility compared to Ceria and high catalytic activity for partial oxidation towards hydrocarbons. This material is yet to be tested in SOFC environment with Platinum metal. Introduction of cobalt was claimed to improve the thermal stability of the Cu-based cermets in CO fuels compared to H{sub}2 at 8000℃, producing the power densities of 310 mW cm{sup}(-2) in H{sub}2 and 370 mW cm{sup}(-2) in CO. Mixed-conductors are the subject of most active researches and the prominent materials so far investigated are Zr/Ti/Y/O, La/Cr/O, La/Sr/Co/Fe/O, La/Sr/Cr/V/O, La/F e/Y/Sr/Ti/O, La/Sr/Cr/NiO etc. These compositions were studied as novel anodes but somehow produced less catalytic activity compared to that of Ni composites. With (LSGM) as electrolyte, SrCo{sub}0.8Fe{sub}0.2O{sub}(3-δ) as the cathode and LDC as buffer layer, a porous composite anode of Ni and La-doped ceria exhibited a power density as high as 1.4Wcm{sup}(-2) at 8000℃ in H{sub}2 and seems to be highest so far published in literature at that temperature. In another case, H2S is oxidized by the mixed-valent La{sub}(1-x)Sr{sub}xVO{sub}(3-δ) (LSV) perovskite, which makes an SOFC with LSV- anode tolerant to 10% H{sub}2S in H{sub}2, but the P{sub}(max) generated was far from being competitive. Since Doped Cerias are proved to be tolerant to sulfur poisoning and found to replenish O{sub}2-ions to the reactive surfaces in order to prevent coke buildup; the next prudent and logical step is to explore other oxides that are MIECs in the reducing atmospheres at the anode and are catalytically more active than ceria for hydrocarbons. At this moment, there are a number of potential alternatives to the Ni or Cu-based anodes in the field of 'novel-anode' search. The catalytic activity of most of the promising oxides needs to be elevated with the infiltration/impregnation techniques done at low enough temperatures. The prime intention of this article is to highlight the contribution that materials engineers have made to the efficient development of Anodes of the SOFCs.
机译:固体氧化物燃料电池(SOFC)是电化学装置,与传统的发电资源相比具有明显的优势。尽管具有所有这些牢固的优势,在继续进行固体氧化物燃料电池(SOFC)的商业化之前,仍然有许多障碍需要克服。这些障碍中最重要的主要包括工作温度区域,电极,电解质,互连件的适当材料选择以及组件的兼容性!在这篇综述中,主要评估阳极的材料性能,并探索混合离子电子导体(MIEC)作为最可能的候选材料。概述了对MIEC的不同限制,并描绘了通往改进阳极的可能途径。当前的状况迫使SOFC社区探索能够在阳极处传导离子物种(MIEC)的电子传导复合材料。大多数MIEC钙钛矿通过氧空位促进了氧化物离子的传导,而La {sub}(1-x)Sr {sub} xTiO {sub}(3 +δ)在钙钛矿基体中有一些移动的氧空位。在H {sub} 2中,Sr {sub} 2Mg {sub}(1-x)Mn {sub} xMoO {sub}(6-δ)在8000℃下的离子电导率为〜10 S / cm。耐性和优异的阳极性能。使用La {sub} 0.8Sr {sub} 0.2Ga {sub} 0.83Mg {sub} 0.17O {sub} 2.815(LSGM)作为电解质,SrCo {sub} 0.8Fe {sub} 0.2O {sub}(3- δ)作为系统的阴极,在8000℃时达到的最大功率密度(P {sub}(max))为0.84 Wcm {sup}(-2),在7000℃时达到0.45 Wcm {sup}(-2)。在H {sub} 2中。将Rh作为贵金属添加到Cu / SDC阳极中,可显着提高甲烷中的电池性能。与氧化铈相比,Ce {sub} 0.84Ti {sub} 0.15Pt {sub} 0.01O {sub}(2-δ)表现出良好的还原性,并且对部分氧化成烃具有高催化活性。该材料尚未在SOFC环境中使用铂金属进行测试。据称,钴的引入与8000℃下的H {sub} 2相比,改善了CO燃料中铜基金属陶瓷的热稳定性,在H {sub}中产生了310 mW cm {sup}(-2)的功率密度。 CO中的2和370 mW cm {sup}(-2)。混合导体是最活跃的研究对象,到目前为止,研究的主要材料是Zr / Ti / Y / O,La / Cr / O,La / Sr / Co / Fe / O,La / Sr / Cr / V / O,La / F e / Y / Sr / Ti / O,La / Sr / Cr / NiO等。这些成分被研究为新型阳极,但以某种方式产生的阳极较少与镍复合材料相比具有催化活性。以(LSGM)为电解质,SrCo {sub} 0.8Fe {sub} 0.2O {sub}(3-δ)为阴极,LDC为缓冲层,Ni和La掺杂二氧化铈的多孔复合阳极表现出功率密度在H {sub} 2中,在8000℃时高达1.4Wcm {sup}(-2),似乎是迄今为止在该温度下最高的文献。在另一种情况下,H2S被混合价的La {sub}(1-x)Sr {sub} xVO {sub}(3-δ)(LSV)钙钛矿氧化,这使得具有LSV-阳极耐受性的SOFC达到10在H {sub} 2中占%H {sub} 2S,但是生成的P {sub}(max)远没有竞争力。由于掺杂二氧化铈被证明对硫中毒具有耐受性,并发现其可将O {sub} 2-离子补充至反应性表面,以防止积碳;接下来的审慎而合乎逻辑的步骤是,探索其他氧化物,这些氧化物在阳极的还原气氛中为MIEC,并且对于碳氢化合物而言,其催化活性比二氧化铈更高。目前,在“新颖阳极”搜索领域中,有许多潜在的替代镍或铜基阳极的方法。大多数有希望的氧化物的催化活性需要通过在足够低的温度下完成的渗透/浸渍技术来提高。本文的主要目的是强调材料工程师为SOFC阳极的有效开发做出的贡献。

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